Dersleri yüzünden oldukça stresli bir ruh haline sikiş hikayeleri bürünüp özel matematik dersinden önce rahatlayabilmek için amatör pornolar kendisini yatak odasına kapatan genç adam telefonundan porno resimleri açtığı porno filmini keyifle seyir ederek yatağını mobil porno okşar ruh dinlendirici olduğunu iddia ettikleri özel sex resim bir masaj salonunda çalışan genç masör hem sağlık hem de huzur sikiş için gelip masaj yaptıracak olan kadını gördüğünde porn nutku tutulur tüm gün boyu seksi lezbiyenleri sikiş dikizleyerek onları en savunmasız anlarında fotoğraflayan azılı erkek lavaboya geçerek fotoğraflara bakıp koca yarağını keyifle okşamaya başlar


Rationale for Using Social Media to Collect Patient-Reported Outcomes in Patients with Celiac Disease | OMICS International
ISSN: 2161-069X
Journal of Gastrointestinal & Digestive System

Like us on:

Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on Medical, Pharma, Engineering, Science, Technology and Business

Rationale for Using Social Media to Collect Patient-Reported Outcomes in Patients with Celiac Disease

Park KT1,2*, Merissa Harris3, Nasim Khavari1 and Chaitan Khosla4

1Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA

2Center for Health Policy/Primary Care Outcomes Research, Stanford University, Stanford, CA, USA

3School of Medicine, George Washington University, District of Columbia, USA

4Department of Chemistry and Biochemistry, Stanford University, Stanford, CA, USA

*Corresponding Author:
750 Welch Road, Ste 116
Palo Alto, CA 94304, USA
Tel: 650-723-5070

Received date: December 07, 2013; Accepted date: January 27, 2014; Published date: February 06, 2014

Citation: Park KT, Harris M, Khavari N, Khosla C (2014) Rationale for Using Social Media to Collect Patient-Reported Outcomes in Patients with Celiac Disease. J Gastroint Dig Syst 4:166. doi:10.4172/2161-069X.1000166

Copyright: © 2014 Park KT, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Journal of Gastrointestinal & Digestive System


Patients with celiac disease (CD) are increasingly interconnected through social media, exchanging patient experiences and health-tracking information between individuals through various web-based platforms. Social media represents potentially unique communication interface between gastroenterologists and active social media users – especially young adults and adolescents with celiac disease-regarding adherence to the strict gluten-free diet, gastrointestinal symptoms, and meaningful discussion about disease management. Yet, various social media platforms may be underutilized for research purposes to collect patient-reported outcomes data. In this commentary, we summarize the scientific rationale and potential for future growth of social media in patient-reported outcomes research, focusing on college freshmen with celiac disease as a case study and provide overview of the methodological approach. Finally, we discuss how social media may impact patient care in the future through increasing mobile technology use.


Social media; Social networking; Facebook; Patientreported outcomes; Healthcare; Mobile technology; Quality-of-life

The Case for Social Media in Patient-Reported Outcomes Research

In this age of social media woven into the fabric of our technologydriven world, today’s physicians are re-examining established ideals of patient privacy and professionalism [1,2]. While the rise of social media within patient care raises real concerns, web-based applications – such as Facebook, Twitter, Google+, Doximity, web blogs, instant messaging platforms, and video chat – represent a growing medium for patients to interact with other patients and social media-savvy health care providers. In gastroenterology, the online celiac disease (CD) community is the largest and most established network of patients exchanging ideas and experiences [3,4]. Within reasonable organizational frameworks, the collective voice from the celiac community aims to raise awareness about important health policy issues affecting CD patients, such as dietary adherence to the gluten-free diet and the current dilemma of under diagnosing patients with silent CD [5,6].

Under the auspices of marketing strategy, researchers are gleaning abundant personal information about patients through social media – to no one’s surprise. Yet, physician-led research is slowly acclimating to this new approach to collecting patient-reported data, although some investigators are increasingly open to new ways of collecting data through social media [4,5]. Physicians and researchers in gastroenterology could benefit from a wealth of possibilities through conducting systematic research through online sources. Facebook, for instance, has more than 1 billion active users worldwide who spend nearly an hour online every day [6]. Evidence suggests that the majority of patients want their healthcare providers to incorporate social media in some patient care, including appointment scheduling and reminders, diagnostic test reporting, health information sharing, prescription notifications, and answering general questions [7,8]. In particular, since the average adolescent and young adult patient’s social media use is widely prevalent and willingness to engage providers through social media is generally favorable, our group hypothesized those biopsyconfirmed CD patients in this demographics may be an optimal group to perform a survey study using Facebook.

Our Pilot Experience Collecting Patient Reported- Outcomes on Facebook

Based on visible interest from private biotechnology companies for clinical trials [9] and the National Institutes of Health [10], electronically-collected patient-reported outcomes (PROs) research is arguably one of the promising areas for future growth in clinical research. Given this background, our research group undertook an exploratory initiative using Facebook. Using our celiac center’s Facebook page (, our research group successfully generated de-identified, longitudinal patient data from CD patients. We were granted institutional IRB approval for this prospective, cross-sectional pilot study. Over a 6 month study period, we collected approximately 150 separate survey responses from 32 college freshmen – 16 with CD and 16 age- and gender-matched healthy controls [9]. We aimed to assess changes in quality-of-life (QOL) and CD-related health due to difficulty adhering to a strict GFD during the first semester of college through 3 validated health surveys. At the end of our study, we saw no statistical difference in the QOL or overall health between the two groups. However, our notion was confirmed that de-identified databases for research were possible and reproducible by using Facebook as the primary portal for study participation.

Guiding principles of clinical research applies in-person and in social media. The planning phase is of utmost importance. We found 19 private or institutional celiac groups with an established presence on Facebook, as shown in Table 1 with each group’s total “Likes.” By contacting these groups through Facebook, information about our study was disseminated on many of the organizations’ Facebook page, and they often voluntarily generated separate web-based announcements, listserv emails, and other social media attention (e.g., Twitter) about our initiative. We adhered to a formal patient enrollment process and timeline, where posted electronic surveys on our Facebook page were used to determine study eligibility of potential participants [10]. HIPAA-compliant electronic surveys generated from an institutional survey tool (e.g., Qualtrics) are recommended. Whenever possible, as with any patient-oriented research, privacy and protection of patienthealth information must take priority.

Organization Web Location #Facebook Likes (43,709 total)
National Celiac Foundation 20,203 likes
Celiac Disease Foundation 13,742 likes
Univ of Chicago Celiac Disease Center 12,740 likes
Gluten Intolerance Group of N. Am 8,404 likes
Center for Celiac Research 3,518 likes
Celiac Sprue Association 3,265 likes
Celiac Disease 2,531 likes
American Celiac Disease Alliance 1,792 likes
About Celiac Disease 1,494 likes
Gluten Free Bay 1,413 likes
Celiac Support Group at Boston Children’s Hospital 958 likes
g-free kids 656 likes
Gluten Free Kids 1,207 likes
The Gluten Free Student Cookbook 377 likes
Teens living with Celiac 146 likes
Gluten Free College girl 138 likes
Udi’s Gluten Free College Ambasasdors 92 likes
North Bay Celiac Group 74 likes
Gluten Free College Kid 54 likes

Table 1: Facebook Celiac Groups with “Likes” count as of April 9, 2013.

Mobile Meets Value-Based Care and Patient-Reported Outcomes

There is a gradual but real momentum in clinical research to use PROs whenever possible. Health care is moving towards a value-based system, where improving patient-reported outcomes – such as QOL – are benchmarks of good clinical practice [11]. Therefore, clinical research naturally follows suite. Forward-thinking researchers can keep pace with this trend by realizing that the public has a natural demand for web-based modalities to facilitate patient care and research, especially on mobile devices. Celiac disease patients already utilizing daily social media use, especially among the adolescent and young adult patient population, represent an opportunity for clinician investigators in gastroenterology to gather valuable PROs.

Nearly 75% of all teens across all demographics use the internet from their mobile devices, and the majority of their total internet use is mobile [12]. There are approximately 7,000 (and growing) mobile healthcare applications in the Apple iTunes Healthcare Room. The future of social media seems to have a good foundation in mobile to effectively change the standard face-to-face and paper-trail methods of health care delivery. While increasing public demand will continue to upgrade the provider-patient experience and patient-advocacy interface of social media, effective methods of collecting PROs, on the other hand, may require more systematic collective thinking and future consensus.


KTP is supported by NIH DK094868. The manuscripts contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH.


Post your comment

Share This Article

Article Usage

  • Total views: 14572
  • [From(publication date):
    February-2014 - Apr 14, 2024]
  • Breakdown by view type
  • HTML page views : 10187
  • PDF downloads : 4385